Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
The okaramine family of compounds, a class of alkaloids with broad-spectrum insecticidal activity, has been discovered from species of and . These okaramines, characterized by their complex structures and diverse biological activities, have attracted widespread attention from biologists and chemists. To date, only a few okaramines have been synthesized, notably the highly active okaramines A and B, which feature a polycyclic skeleton, including an azocine ring and an unprecedented 2-dimethyl-3-methyl-azetidine ring. These compounds have not yet been synthesized artificially. Their potent insecticidal activity is due to their selective activation of glutamate-gated chloride channels in invertebrates without affecting human ligand-gated anion channels. They are promising candidates as lead insecticides and merit further research. This review provides an overview of the research progress in the structural characteristics, nuclear magnetic resonance data, biological activity, biosynthesis, and total synthesis of okaramines, offering a framework for the development of novel pesticides.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1021/acs.jafc.4c06492 | DOI Listing |
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